Ambry Genetics, Aliso Viejo, CA, USA.
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Am J Hum Genet. 2024 Nov 7;111(11):2411-2426. doi: 10.1016/j.ajhg.2024.08.022. Epub 2024 Sep 23.
The ClinGen Hereditary Breast, Ovarian, and Pancreatic Cancer (HBOP) Variant Curation Expert Panel (VCEP) is composed of internationally recognized experts in clinical genetics, molecular biology, and variant interpretation. This VCEP made specifications for the American College of Medical Genetics and Association for Molecular Pathology (ACMG/AMP) guidelines for the ataxia telangiectasia mutated (ATM) gene according to the ClinGen protocol. These gene-specific rules for ATM were modified from the ACMG/AMP guidelines and were tested against 33 ATM variants of various types and classifications in a pilot curation phase. The pilot revealed a majority agreement between the HBOP VCEP classifications and the ClinVar-deposited classifications. Six pilot variants had conflicting interpretations in ClinVar, and re-evaluation with the VCEP's ATM-specific rules resulted in four that were classified as benign, one as likely pathogenic, and one as a variant of uncertain significance (VUS) by the VCEP, improving the certainty of interpretations in the public domain. Overall, 28 of the 33 pilot variants were not VUS, leading to an 85% classification rate. The ClinGen-approved, modified rules demonstrated value for improved interpretation of variants in ATM.
ClinGen 遗传性乳腺癌、卵巢癌和胰腺癌 (HBOP) 变异物管理专家小组 (VCEP) 由在临床遗传学、分子生物学和变异物解读方面具有国际公认专业知识的专家组成。该 VCEP 根据 ClinGen 方案为美国医学遗传学学院和分子病理学协会 (ACMG/AMP) 关于共济失调毛细血管扩张突变基因 (ATM) 的指南制定了规范。这些针对 ATM 的特定基因规则是根据 ACMG/AMP 指南进行修改的,并在试点管理阶段针对各种类型和分类的 33 个 ATM 变体进行了测试。试点揭示了 HBOP VCEP 分类和 ClinVar 存储的分类之间的多数一致性。ClinVar 中有 6 个试点变体的解释存在冲突,根据 VCEP 的 ATM 特定规则重新评估后,其中 4 个被归类为良性,1 个被归类为可能致病性,1 个被归类为意义不明的变异 (VUS),从而提高了公共领域解释的确定性。总体而言,33 个试点变体中没有 28 个是 VUS,分类率为 85%。经 ClinGen 批准的修改规则证明对 ATM 中变异物的解释具有改进价值。